ANOMALIAS CROMOSOMICAS PDF

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31 May Transcript of ANOMALIAS CROMOSÓMICAS. En el 95 % de los casos está causado por una trisomía del cromosoma 21 debida a una no. 29 Oct Transcript of Anomalias Cromosomicas. Capitulo 1. Capitulo 3. ANOMALIAS DETECTADAS EN BOGOTÁ LOS ULTIMOS 10 AÑOS. IX. Anomalías cromosómicas. A. Anomalías numéricas 3. anomalías menores 4. enfermedad cardiaca congénita 5. atresia duodenal 6. retraso mental.

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Am J Hum Genet, 39pp. Present to your audience Start remote presentation.

Clinical significance and distribution of break points. Cytogenetic and molecular analysis of trisomy 9. Cytogenet Cell Genet, 41pp. Cytogenetic analysis of blast cells in childhood acute lymphoblastic leukemia has led to the recognition of specific non-random chromosomal abnormalities with prognostic value.

ANOMALIAS CROMOSÓMICAS by Daniel Redrobán on Prezi

More presentations by valentina vasquez Propuesta de desarrollo de un acuario au Internal intersexuality masculine uterus and severe abnormality of the anterior chamber of the eye. J Med Genet, 31pp. Am J Med Genet, 69pp. Neither you, nor the coeditors you shared it with will be able to recover it again.

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Clases de citogenética de Dinulos — 2.ª parte

Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence. Hum Genet, 80pp. Prenat Diagn, 9pp. Prenatal diagnosis of a new family and brief review. Are you a health professional able to prescribe or dispense drugs? It is important to determine anlmalias risk to provide patients with appropriate genetic counseling. Risk of phenotypic abnormalities in paracentric inversion carriers.

crojosomicas Translocation t 1;5 q21;p13 in a male with azoospermia. Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection. Urol Int, 44pp.

Non C-banding variants in some normal families might be homogeneously staining regions.

Citogenética Clínica

Hum Genet, 76pp. La persona puede tener cromosomas XX, cromosomas XY o ambos.

Heritable deletion of band 16q21 with normal phenotype: A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup 15 marker chromosomes. Ann Genet, 34pp. Chromosome abnormalities found among newborn children: Hum Genet, 71pp. Am J Med Genet, 61 cromosomixas, pp. Uniparental disomy 16 in association with congenital heart disease. Present to your audience Start remote presentation.

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Stand out and be remembered with Prezi, the secret weapon of great presenters. Am J Med Genet, 36pp. Please log in anpmalias add your comment.

Author links open overlay panel M. This study focuses on the most important chromosomal abnormalities found in childhood ALL and their prognostic and therapeutic implications. J Med Genet, 38pp.